Senior Medical Writer - Global Clinical Research Organisation - Home based in UK

JR United Kingdom; Exeter; Remote; GBP 45,000 - 65,000; Full time

Job summary

A global clinical research organisation is seeking a Senior Medical Writer for a home-based position in Exeter. This role involves authoring complex clinical documents and leading medical writing projects, offering an exciting opportunity to impact key therapies in various therapeutic areas.

Qualifications

• Experience as a medical writer and project lead on medical writing projects.
• Experience with Phase I - III protocol and CSR medical writing.
• Strong project management and leadership skills.

Responsibilities

• Author high-complexity study-level documents including protocols and investigator brochures.
• Independently author clinical evaluation plans and reports, and global regulatory submissions.
• Supervise and guide junior medical writers.

Skills

Medical Writing

Project Management

Stakeholder Management

Leadership

Job description

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Senior Medical Writer - Global Clinical Research Organisation - Home based in UK, Exeter

Client: Planet Pharma

Location: Exeter, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

1

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

Senior Medical Writer - Global Clinical Research Organisation - Home based in UK

Planet Pharma is currently working with a global clinical research organisation (CRO) that is looking for an experienced Medical Writer to join their team and support the preparation of submission and other complex clinical documents.

As a Senior Medical Writer, you will be responsible for authoring high-complexity study-level documents including protocols, ICFs, investigator brochures, and meeting packages. You will also independently author:

• Clinical evaluation plans and reports
• Paediatric Investigational Plans (PIPs)
• Clinical summary and overview documents in CTD/eCTD formats for global regulatory submissions

This is an exciting opportunity to join a globally renowned CRO and contribute significantly to bringing key therapies to market across various therapeutic areas. You will be assigned to one sponsor, leading multiple projects, and supervising and guiding junior medical writers.

For this position, the client seeks someone with experience as a medical writer and project lead on medical writing projects.

Additionally, candidates should have experience with:

• Phase I - III protocol and CSR medical writing
• Stakeholder management, both internal and external
• Project management and leadership skills

For more information or similar opportunities, please contact Chanel Hicken at 0203 868 1011 or email your updated CV to [emailprotected]. We can arrange a confidential discussion on how you can get involved in this exciting role.